Atlas FDA

CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY

FDA 510(k) clearance K901374 · decided 1990-06-26

Clearance details

K-number
K901374
Device name
CENTREMARK(TM) CENTRAL VENOUS CATHETER TRAY
Applicant
Menlo Care, Inc.
Decision
Unknown
Date received
1990-03-22
Decision date
1990-06-26
Days to decision
96 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Palo Alto, CA, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.